Department of Chemistry and Green-Nano Materials Research Center, Kyungpook National University, Daegu 702-701, Republic of Korea.
J Hazard Mater. 2012 Oct 30;237-238:180-5. doi: 10.1016/j.jhazmat.2012.08.025. Epub 2012 Aug 19.
Porous metal-organic frameworks (MOFs, MIL-100-Fe, iron-benzenetricarboxylate) supported with Cu(+) species were obtained for the first time under mild condition without high temperature calcinations. The Cu(+)-loaded MOFs were evaluated as efficient adsorbents for the liquid-phase adsorption of benzothiophene (BT). The effect of Cu(+) loading on the adsorption kinetics and maximum adsorption capacity (Q(0)) for the adsorption of BT was also studied. Q(0) increased with increasing copper loading up to a Cu/Fe (wt./wt.) ratio of 0.07 in Cu(+)-loaded-MIL-100-Fe, resulting in an increase in the Q(0) by 14% compared with the virgin MIL-100-Fe without Cu(+) ions. Since the surface area and pore volume decrease with the loading of copper, the increased Q(0) over the Cu(+)-loaded MIL-100-Fe adsorbents suggests specific favorable interactions (probably by π-complexation) between Cu(+) and BT.
首次在温和条件下(无需高温煅烧)制备了负载 Cu(+) 的多孔金属有机骨架(MOFs,MIL-100-Fe,铁-均苯三甲酸)。将负载 Cu(+) 的 MOFs 作为液相吸附苯并噻吩(BT)的有效吸附剂进行了评价。还研究了 Cu(+) 负载量对 BT 吸附动力学和最大吸附容量(Q(0))的影响。Cu(+)-负载 MIL-100-Fe 中的 Q(0) 随铜负载量的增加而增加,在 Cu/Fe(质量/质量)比为 0.07 时达到最大值,与不含 Cu(+) 离子的原始 MIL-100-Fe 相比,Q(0) 增加了 14%。由于负载铜后表面积和孔体积减小,Cu(+)-负载 MIL-100-Fe 吸附剂上 Q(0) 的增加表明 Cu(+) 和 BT 之间存在特定的有利相互作用(可能是通过π 络合)。